TECHNICAL FIELD
[0001] The present disclosure relates to a non-aqueous electrolyte secondary battery.
BACKGROUND
[0002] In recent years, as a secondary battery having high output and high energy density,
a non-aqueous electrolyte secondary battery that includes a positive electrode, a
negative electrode, and a non-aqueous electrolyte and performs charging and discharging
by moving lithium ions and the like between the positive electrode and the negative
electrode has been widely used.
[0003] For example, Patent Literature 1 discloses a non-aqueous electrolyte secondary battery
including a positive electrode material in which barium titanate as a dielectric is
present on a surface of a positive electrode active material. In the non-aqueous electrolyte
secondary battery disclosed in Patent Literature 1, it is described that interface
resistance is reduced by the presence of barium titanate on the surface of the positive
electrode active material.
CITATION LIST
PATENT LITERATURE
SUMMARY
[0005] When the dielectric and the positive electrode active material are mixed in manufacturing
the positive electrode, the dielectrics may be aggregated and not uniformly dispersed.
Since the dielectric itself has an insulating property, for example, in a battery
including a positive electrode in which dielectrics are unevenly distributed, charge
transfer resistance may increase.
[0006] An object of the present disclosure is to provide a non-aqueous electrolyte secondary
battery having low charge transfer resistance.
[0007] A non-aqueous electrolyte secondary battery according to an aspect of the present
disclosure includes a positive electrode, a negative electrode, and a non-aqueous
electrolyte, in which the positive electrode includes a positive electrode current
collector and a positive electrode mixture layer provided on the positive electrode
current collector, the positive electrode mixture layer includes a positive electrode
active material and a dielectric, and a ratio (D50 of the dielectric/D50 of the positive
electrode active material) of a volume-based median diameter (D50) of the dielectric
to a volume-based median diameter (D50) of the positive electrode active material
is greater than or equal to 0.15 and less than or equal to 0.6.
[0008] According to an aspect of the present disclosure, it is possible to provide a non-aqueous
electrolyte secondary battery having low charge transfer resistance.
BRIEF DESCRIPTION OF DRAWINGS
[0009]
FIG. 1 is a cross-sectional view of a non-aqueous electrolyte secondary battery as
an example of an embodiment.
FIG. 2 is a view showing a relative value of charge transfer resistance of each of
batteries of Examples and other Comparative Examples when the charge transfer resistance
of the battery of Comparative Example 1 is 1.
DESCRIPTION OF EMBODIMENTS
[0010] Hereinafter, examples of embodiments will be described in detail. The drawings referred
to in the description of the embodiment are schematically illustrated, and dimensional
ratios and the like of components drawn in the drawings may be different from actual
ones.
[0011] FIG. 1 is a cross-sectional view of a non-aqueous electrolyte secondary battery as
an example of an embodiment. A non-aqueous electrolyte secondary battery 10 illustrated
in FIG. 1 includes a wound electrode assembly 14 formed by wounding a positive electrode
11 and a negative electrode 12 with a separator 13 interposed between the positive
electrode 11 and the negative electrode 12, a non-aqueous electrolyte, insulating
plates 18 and 19 that are disposed on upper and lower sides of the electrode assembly
14, respectively, and a battery case housing the members and including a case body
16 and a sealing assembly 17. Note that, instead of the wound electrode assembly 14,
another form of an electrode assembly such as a stacked electrode assembly in which
a positive electrode and a negative electrode are alternately stacked with a separator
interposed therebetween may be applied. In addition, examples of the battery case
include a metal case having a cylindrical shape, a square shape, a coin shape, a button
shape, or the like, and a resin case formed by laminating resin sheets (so-called
laminate type resin case).
[0012] The case body 16 is, for example, a bottomed cylindrical metal container. A gasket
28 is provided between the case body 16 and the sealing assembly 17 to secure a sealing
property of the inside of the battery. The case body 16 has, for example, a projecting
portion 22 in which a part of a side part thereof projects inside for supporting the
sealing assembly 17. The projecting portion 22 is preferably formed in an annular
shape along a circumferential direction of the case body 16, and supports the sealing
assembly 17 on an upper surface thereof.
[0013] The sealing assembly 17 has a structure in which a filter 23, a lower vent member
24, an insulating member 25, an upper vent member 26, and a cap 27 are sequentially
stacked from the electrode assembly 14. Each member constituting the sealing assembly
17 has, for example, a disk shape or a ring shape, and the respective members except
for the insulating member 25 are electrically connected to each other. The lower vent
member 24 and the upper vent member 26 are connected to each other at the respective
central parts thereof, and the insulating member 25 is interposed between the respective
circumferential parts of the vent members 24 and 26. When the internal pressure of
the non-aqueous electrolyte secondary battery 10 is increased by heat generation due
to an internal short circuit or the like, for example, the lower vent member 24 is
deformed so as to push the upper vent member 26 up toward the cap 27 side and is broken,
and thus, a current pathway between the lower vent member 24 and the upper vent member
26 is cut off. When the internal pressure is further increased, the upper vent member
26 is broken, and gas is discharged through an opening of the cap 27.
[0014] In the non-aqueous electrolyte secondary battery 10 illustrated in FIG. 1, a positive
electrode lead 20 attached to the positive electrode 11 extends through a through-hole
of the insulating plate 18 toward a side of the sealing assembly 17, and a negative
electrode lead 21 attached to the negative electrode 12 extends through the outside
of the insulating plate 19 toward the bottom side of the case body 16. The positive
electrode lead 20 is connected to a lower surface of the filter 23 that is a bottom
plate of the sealing assembly 17 by welding or the like, and the cap 27 that is a
top plate of the sealing assembly 17 electrically connected to the filter 23 becomes
a positive electrode terminal. The negative electrode lead 21 is connected to a bottom
inner surface of the case body 16 by welding or the like, and the case body 16 becomes
a negative electrode terminal.
[Positive Electrode]
[0015] The positive electrode 11 includes a positive electrode current collector and a positive
electrode mixture layer disposed on the positive electrode current collector. Note
that the positive electrode mixture layer is desirably disposed on both surfaces of
the positive electrode current collector.
[0016] As the positive electrode current collector, a foil of a metal stable in a potential
range of the positive electrode, such as aluminum or an aluminum alloy, a film in
which the metal is disposed on a surface layer, or the like can be used. The positive
electrode current collector has a thickness of, for example, about greater than or
equal to 10 µm and less than or equal to 100 µm.
[0017] The positive electrode mixture layer includes a positive electrode active material
and a dielectric. It is preferable that the positive electrode mixture layer includes
a binder from the viewpoint of binding the positive electrode active materials to
each other to secure the mechanical strength of the positive electrode mixture layer.
In addition, it is preferable that the positive electrode mixture layer includes a
conductive agent from the viewpoint of improving the conductivity of the layer.
[0018] The positive electrode 11 is manufactured, for example, as follows. First, a positive
electrode active material, a dielectric, a binder, a conductive agent, and the like
are mixed, and the mixture is dispersed in a solvent to prepare a positive electrode
mixture slurry. Then, the positive electrode mixture slurry is applied onto the positive
electrode current collector, a coating film is dried, and then the coating film is
rolled, such that the positive electrode 11 can be manufactured.
[0019] A ratio (D50 of the dielectric/D50 of the positive electrode active material) of
a volume-based median diameter (D50) of the dielectric to a volume-based median diameter
(D50) of the positive electrode active material is greater than or equal to 0.15 and
less than or equal to 0.6 and preferably greater than or equal to 0.26 and less than
or equal to 0.45. As described above, when the dielectric and the positive electrode
active material are mixed in manufacturing the positive electrode, the dielectrics
may be unevenly distributed. Since the dielectric itself has an insulating property,
when the dielectrics are unevenly distributed in the positive electrode mixture layer,
the charge transfer resistance of the battery may increase. However, when D50 of the
dielectric/D50 of the positive electrode active material is within the above range,
it is presumed that uneven distribution of the dielectrics is suppressed and the dielectrics
are dispersed in the positive electrode mixture layer on average to some extent as
compared with the case outside the above range. As a result, for example, it is considered
that lithium ions in the non-aqueous electrolyte are attracted to the vicinity of
the positive electrode active material by dielectric polarization of the dielectric,
occlusion and release of the lithium ions in the positive electrode active material
are promoted, and the charge transfer resistance of the battery is reduced.
[0020] In the present disclosure, the volume-based median diameter (D50) means a particle
diameter at which a cumulative frequency is 50% from a smaller particle diameter side
in a particle size distribution on a volumetric basis, and is also called a median
diameter. The particle diameter and particle size distribution of the positive electrode
active material or the dielectric can be measured by a laser diffraction type particle
size distribution measuring device (for example, MT3000II, manufactured by MicrotracBEL
Corp.).
[0021] The volume-based median diameter (D50) of the positive electrode active material
is preferably greater than or equal to 5 µm and less than or equal to 20 µm and more
preferably greater than or equal to 8 µm and less than or equal to 18 µm from the
viewpoint of further reducing the charge transfer resistance of the battery.
[0022] The positive electrode active material is not particularly limited as long as it
is a lithium composite oxide capable of reversibly inserting and removing lithium,
but for example, it is preferable to include a lithium composite oxide represented
by the following General Formula (1) from the viewpoint of an increase in capacity
of the battery, excellent charge and discharge cycle characteristics, and the like.
Li
aNi
bCo
(1-b-c)Al
cW
dO
e (1)
[0023] In the formula, 0.9 < a ≤ 1.2, 0.88 ≤ b ≤ 0.96, 0.04 ≤ c ≤ 0.12, and 1.9 ≤ e ≤ 2.1,
and when W/(Ni + Co + Al + W) = d, it is preferable that 0.0003 ≤ d ≤ 0.002. The composition
of the lithium composite oxide can be measured by inductively coupled plasma (ICP)
emission spectrometry.
[0024] The dielectric is a substance that is excellent in dielectric properties than conductivity
and can be said to be an insulator against a DC voltage. Examples of the dielectric
include a composite oxide having any one of crystal structures of XYO
3 type, X
2Y
2O
7 type, and XX'
3Y
4O
12 type. X is one or two or more elements of an alkali metal element (for example, elements
in Group 1 such as Na, K, Rb, and Cs), an alkaline earth metal element (for example,
elements in Group 2 such as Ca, Sr, and Ba), a rare earth metal element (for example,
La, Ce, Nd, Sm, Gd, Yb, and the like), Cu, Pb, and Bi. X' is, for example, one or
two or more elements of transition metal elements, and is an element different from
X. Y is one or two or more elements of transition metal elements and Sn. The transition
metal element is, for example, an element belonging to Groups 3 to 11 of IUPAC classification.
Examples thereof include elements in Group 4 (for example, Ti, Zr, Hf, and the like),
elements in Group 5 (for example, V, Nb, Ta, and the like), elements in Group 6 (Cr,
Mo, W, and the like), elements in Group 7 (Mn, Tc, and the like), elements in Group
8 (Fe, Ru, Os, and the like), elements in Group 9 (Co, Rh, Ir, and the like), elements
in Group 10 (Ni, Pd, Pt, and the like), elements in Group 11 (Cu, Ag, Au, and the
like), and rare earth metal elements (La, Ce, Sm, and the like). In addition, Y preferably
includes an element different from X, and more preferably consists of an element different
from X. Examples of particularly preferred dielectric include BaTiO
3. Note that the crystal structure of the dielectric can be confirmed by XRD measurement
using a CuKα ray.
[0025] A relative permittivity of the dielectric is preferably greater than or equal to
8 and less than or equal to 500 and more preferably greater than or equal to 50 and
less than or equal to 500. In addition, a volume resistivity at 20°C is preferably
greater than or equal to 1 × 10
5 Ω·m, more preferably greater than or equal to 1 × 10
6 Ω·m, and still more preferably greater than or equal to 1 × 10
10 Ω·m.
[0026] A content of the dielectric is, for example, preferably less than or equal to 2%
by mass, and preferably less than or equal to 1% by mass, with respect to the mass
of the positive electrode active material. When the content of the dielectric is greater
than 2% by mass with respect to the mass of the positive electrode active material,
the capacity of the battery may be reduced as compared with the case of less than
or equal to 2% by mass. A lower limit value of the content of the dielectric is not
particularly limited, and may be, for example, greater than or equal to 0.1% by mass
with respect to the mass of the positive electrode active material from the viewpoint
of effectively reducing the charge transfer resistance of the battery.
[0027] Examples of the conductive agent contained in the positive electrode mixture layer
include carbon materials such as carbon black, acetylene black, Ketjenblack, and graphite.
These conductive agents may be used alone or in combination of two or more thereof.
A content of the conductive agent in the positive electrode mixture layer is, for
example, preferably greater than or equal to 0.5% by mass and less than or equal to
4% by mass, and more preferably greater than or equal to 0.5% by mass and less than
or equal to 1.5% by mass.
[0028] Examples of the binder contained in the positive electrode mixture layer include
a fluororesin such as polytetrafluoroethylene (PTFE) or polyvinylidene fluoride (PVdF),
polyacrylonitrile (PAN), a polyimide-based resin, an acrylic resin, a polyolefin-based
resin, styrene-butadiene rubber (SBR), carboxymethyl cellulose (CMC) or a salt thereof,
polyacrylic acid (PAA) or a salt thereof (PAA-Na, PAA-K, and the like, or a partially
neutralized salt may be used), polyethylene oxide (PEO), and polyvinyl alcohol (PVA).
These conductive agents may be used alone or in combination of two or more thereof.
A content of the binder in the positive electrode mixture layer is, for example, preferably
greater than or equal to 0.5% by mass and less than or equal to 4% by mass, and more
preferably greater than or equal to 0.5% by mass and less than or equal to 1.5% by
mass.
[Negative Electrode]
[0029] The negative electrode 12 includes, for example, a negative electrode current collector
and a negative electrode mixture layer formed on the current collector. As the negative
electrode current collector, a foil of a metal stable in a potential range of the
negative electrode, such as copper, a film in which the metal is disposed on a surface
layer, or the like can be used. The negative electrode mixture layer includes, for
example, a negative electrode active material, a binder, and the like. The negative
electrode 12 can be manufactured, for example, as follows. First, a negative electrode
active material, a binder, and the like are mixed, and the mixture is dispersed in
a solvent to prepare a negative electrode mixture slurry. The negative electrode mixture
slurry is applied onto the negative electrode current collector, a coating film is
dried, and then the coating film is rolled, such that the negative electrode 12 can
be manufactured.
[0030] The negative electrode active material is not particularly limited as long as it
is a material capable of occluding and releasing lithium ions, and examples thereof
include a lithium alloy such as metal lithium, a lithium-aluminum alloy, a lithium-lead
alloy, a lithium-silicon alloy, or a lithium-tin alloy, a carbon material such as
graphite, coke, or an organic substance baked body, and a metal oxide such as SnO
2, SnO, or TiO
2. These materials may be used alone or in combination of two or more thereof.
[0031] Examples of the binder contained in the negative electrode mixture layer include
a fluorine-based resin, PAN, a polyimide-based resin, an acrylic resin, a polyolefin-based
resin, SBR, CMC or a salt thereof, PAA or a salt thereof, PEO, and PVA as in the case
of the positive electrode. Note that the negative electrode mixture layer may include
a conductive agent as in the case of the positive electrode.
[Separator]
[0032] For example, a porous sheet having an ion permeation property and an insulation property
is used for the separator 13. Specific examples of the porous sheet include a fine
porous thin film, a woven fabric, and a non-woven fabric. The separator 13 is formed
of, for example, a polyolefin such as polyethylene or polypropylene, or cellulose.
The separator 13 may be a laminate including a cellulose fiber layer and a thermoplastic
resin fiber layer formed of a polyolefin or the like. In addition, the separator 13
may be a multi-layer separator including a polyethylene layer and a polypropylene
layer, and may have a surface layer formed of an aramid resin or a surface layer including
an inorganic filler.
[Non-Aqueous Electrolyte]
[0033] The non-aqueous electrolyte contains a non-aqueous solvent and an electrolyte salt.
As the non-aqueous solvent, for example, esters, ethers, nitriles such as acetonitrile,
amides such as dimethylformamide, a mixed solvent of two or more thereof, and the
like can be used. The non-aqueous solvent may contain a halogen-substituted product
in which at least some hydrogens in these solvents are substituted with halogen atoms
such as fluorine.
[0034] Examples of the esters include cyclic carbonates such as ethylene carbonate (EC),
propylene carbonate (PC), and butylene carbonate, chain carbonic acid esters such
as dimethyl carbonate (DMC), methyl ethyl carbonate (MEC), diethyl carbonate (DEC),
methyl propyl carbonate, ethyl propyl carbonate, and methyl isopropyl carbonate, cyclic
carboxylic acid esters such as γ-butyrolactone and γ-valerolactone, and chain carboxylic
acid esters such as methyl acetate, ethyl acetate, propyl acetate, methyl propionate
(MP), and ethyl propionate.
[0035] Examples of the ethers include cyclic ethers such as 1,3-dioxolane, 4-methyl-1,3-dioxolane,
tetrahydrofuran, 2-methyltetrahydrofuran, propylene oxide, 1,2-butylene oxide, 1,3-dioxane,
1,4-dioxane, 1,3,5-trioxane, furan, 2-methylfuran, 1,8-cineole, and crown ether, and
chain ethers such as 1,2-dimethoxyethane, diethyl ether, dipropyl ether, diisopropyl
ether, dibutyl ether, dihexyl ether, ethyl vinyl ether, butyl vinyl ether, methyl
phenyl ether, ethyl phenyl ether, butyl phenyl ether, pentyl phenyl ether, methoxytoluene,
benzyl ethyl ether, diphenyl ether, dibenzyl ether, o-dimethoxybenzene, 1,2-diethoxyethane,
1,2-dibutoxyethane, diethylene glycol dimethyl ether, diethylene glycol diethyl ether,
diethylene glycol dibutyl ether, 1,1-dimethoxymethane, 1,1-diethoxyethane, triethylene
glycol dimethyl ether, and tetraethylene glycol dimethyl ether.
[0036] Examples of the nitriles include acetonitrile, propionitrile, butyronitrile, valeronitrile,
n-heptanonitrile, succinonitrile, glutaronitrile, adiponitrile, pimelonitrile, 1,2,3-propane
tricarbonitrile, and 1,3,5-pentane tricarbonitrile.
[0037] Examples of the halogen-substituted product include fluorinated cyclic carbonic acid
ester such as fluoroethylene carbonate (FEC), fluorinated chain carbonic acid ester,
and fluorinated chain carboxylic acid ester such as methyl fluoropropionate (FMP).
[0038] Examples of the electrolyte salt include borates such as LiBF
4, LiClO
4, LiPF
6, LiAsF
6, LiSbF
6, LiAlCl
4, LiSCN, LiCF
3SO
3, LiCF
3CO
2, Li(P(C
2O
4)F
4), LiPF
6-x(C
nF
2n+1)
x (1 < x < 6, n is 1 or 2), LiB
10Cl
10, LiCl, LiBr, LiI, lithium chloroborane, lithium lower aliphatic carboxylate, Li
2B
4O
7, and Li(B(C
2O
4)F
2), and imide salts such as LiN(SO
2CF
3)
2 and LiN(C
lF
2l+1SO
2)(C
mF
2m+1SO
2) {l and m are integers greater than or equal to 1}. These electrolyte salts may be
used alone or in combination of a plurality of kinds thereof. A concentration of the
electrolyte salt is, for example, greater than or equal to 0.8 mol and less than or
equal to 1.8 mol per 1 L of the non-aqueous solvent.
EXAMPLES
[0039] Hereinafter, the present disclosure will be further described with reference to Examples,
but the present disclosure is not limited to these Examples.
<Example 1>
[Preparation of Positive Electrode Active Material]
[0040] Particles of a lithium composite oxide A having a layered structure represented by
LiNi
0.91Co
0.04Al
0.05O
2 and tungsten oxide (WO
3) were mixed at a predetermined ratio, and then heat-treated to obtain a lithium composite
oxide B containing a tungsten compound. The lithium composite oxide B was used as
a positive electrode active material. The volume-based median diameter (D50) of the
positive electrode active material was 12.0 µm. Note that the amount of the tungsten
compound added was 0.08 atom% in terms of tungsten element with respect to the total
molar amount of metal elements excluding lithium in the lithium composite oxide A.
[Manufacture of Positive Electrode]
[0041] 100 parts by mass of a positive electrode active material, 1 part by mass of acetylene
black as a conductive agent, 1 part by mass of polyvinylidene fluoride as a binder,
and 0.3 parts by mass of barium titanate (BaTiO
3) having a volume-based median diameter (D50) of 3.8 µm were mixed, and then an appropriate
amount of N-methyl-2 pyrrolidone (NMP) was added, thereby preparing a positive electrode
mixture slurry. The slurry was applied onto both surfaces of a positive electrode
current collector formed of an aluminum foil, the coating film was dried, and then
the coating film was rolled by a rolling roller, thereby manufacturing a positive
electrode in which a positive electrode mixture layer was formed on both surfaces
of a positive electrode current collector.
[Manufacture of Negative Electrode]
[0042] 95 parts by mass of a negative electrode active material formed of graphite powder
and silicon oxide, 3 parts by mass of carboxymethyl cellulose (CMC), 2 parts by mass
of styrene-butadiene rubber (SBR), and an appropriate amount of water were mixed,
thereby preparing a negative electrode mixture slurry. The slurry was applied onto
both surfaces of a negative electrode current collector formed of a copper foil, the
coating film was dried, and then the coating film was rolled by a rolling roller,
thereby manufacturing a negative electrode in which a negative electrode mixture layer
was formed on both surfaces of a negative electrode current collector.
[Preparation of Non-Aqueous Electrolyte]
[0043] LiPF
6 was dissolved at a concentration of 1.0 mol/L in a mixed non-aqueous solvent of ethylene
carbonate (EC) and methyl ethyl carbonate (MEC) to obtain a non-aqueous electrolyte.
[Manufacture of Non-Aqueous Electrolyte Secondary Battery]
[0044] A positive electrode lead was attached to the manufactured positive electrode, and
a negative electrode lead was attached to the manufactured negative electrode. A polyethylene
microporous film as a separator was disposed between both electrodes and wound in
a spiral shape to produce a wound electrode assembly. The electrode assembly and the
non-aqueous electrolyte were disposed in an exterior body of an aluminum laminate,
and then a peripheral edge of the exterior body was heated and welded to obtain a
non-aqueous electrolyte secondary battery.
<Example 2>
[0045] A non-aqueous electrolyte secondary battery was manufactured in the same manner as
that of Example 1, except that the amount of barium titanate (BaTiO
3) was set to 0.5 parts by mass.
<Example 3>
[0046] A non-aqueous electrolyte secondary battery was manufactured in the same manner as
that of Example 1, except that barium titanate (BaTiO
3) having a volume-based median diameter (D50) of 5.4 µm was used.
<Example 4>
[0047] A non-aqueous electrolyte secondary battery was manufactured in the same manner as
that of Example 1, except that barium titanate (BaTiO
3) having a volume-based median diameter (D50) of 3.1 µm was used.
<Example 5>
[0048] A non-aqueous electrolyte secondary battery was manufactured in the same manner as
that of Example 1, except that barium titanate (BaTiO
3) having a volume-based median diameter (D50) of 2.2 µm was used.
<Comparative Example 1>
[0049] A non-aqueous electrolyte secondary battery was manufactured in the same manner as
that of Example 1, except that barium titanate (BaTiO
3) was not added.
<Comparative Example 2>
[0050] A non-aqueous electrolyte secondary battery was manufactured in the same manner as
that of Example 1, except that barium titanate (BaTiO
3) having a volume-based median diameter (D50) of 10.0 µm was used.
<Comparative Example 3>
[0051] A non-aqueous electrolyte secondary battery was manufactured in the same manner as
that of Example 1, except that barium titanate (BaTiO
3) having a volume-based median diameter (D50) of 1.2 µm was used.
[Measurement of Charge Transfer Resistance]
[0052] Each of the non-aqueous secondary batteries of Examples and Comparative Examples
was subjected to constant current charge at a constant current of 0.2 C until a battery
voltage reached 4.2 V under a temperature environment at 25°C. For these non-aqueous
electrolyte secondary batteries, alternating current impedance measurement was performed
in a range of 0.1 Hz to 1 kHz to create a Cole-Cole plot. The charge transfer resistance
of the battery was determined from a diameter of a substantially semicircle appearing
in the obtained Cole-Cole plot. The charge transfer resistance of the battery of Comparative
Example 1 was set as 1, and the charge transfer resistance of each of the batteries
of Examples and other Comparative Examples was calculated as a relative value (INDEX).
The results are shown in Table 1 and FIG. 2.
[Table 1]
|
Dielectric BaTiO3 |
Dielectric D50/positive electrode active material D50 |
Charge transfer resistance of battery (Relative value) |
D50 µm |
Content |
Example 1 |
3.8 |
0.3 wt% |
0.32 |
0.88 |
Example 2 |
3.8 |
0.5 wt% |
0.32 |
0.85 |
Example 3 |
5.4 |
0.3 wt% |
0.45 |
0.90 |
Example 4 |
3.1 |
0.3 wt% |
0.26 |
0.94 |
Example 5 |
2.2 |
0.3 wt% |
0.18 |
0.97 |
Comparative Example 1 |
- |
- |
- |
1.00 |
Comparative Example 2 |
10.0 |
0.3 wt% |
0.83 |
1.01 |
Comparative Example 3 |
1.2 |
0.3 wt% |
0.10 |
1.14 |
[0053] As in Examples 1 to 5, when the ratio (D50 of the dielectric/D50 of the positive
electrode active material) of the volume-based median diameter (D50) of the dielectric
to the volume-based median diameter (D50) of the positive electrode active material
was in the range of greater than or equal to 0.15 and less than or equal to 0.6, the
charge transfer resistance of the battery was suppressed to be lower than that in
Comparative Example 1. On the other hand, as in Comparative Examples 2 and 3, when
the ratio (D50 of the dielectric/D50 of the positive electrode active material) of
the volume-based median diameter (D50) of the dielectric to the volume-based median
diameter (D50) of the positive electrode active material was in the range of greater
than or equal to 0.15 and less than or equal to 0.6, the charge transfer resistance
of the battery was suppressed to be higher than that in Comparative Example 1.
REFERENCE SIGNS LIST
[0054]
- 10
- Non-aqueous electrolyte secondary battery
- 11
- Positive electrode
- 12
- Negative electrode
- 13
- Separator
- 14
- Electrode assembly
- 16
- Case body
- 17
- Sealing assembly
- 18, 19
- Insulating plate
- 20
- Positive electrode lead
- 21
- Negative electrode lead
- 22
- Projecting portion
- 23
- Filter
- 24
- Lower vent member
- 25
- Insulating member
- 26
- Upper vent member
- 27
- Cap
- 28
- Gasket